Canonical Allele Identifier:
CA2700303892
Gene:
Linked Data
dbSNP Id:
rs2104681492
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122368769G>A , CM000664.2:g.122368769G>A | GRCh38 |
| NC_000002.11:g.123126345G>A , CM000664.1:g.123126345G>A | GRCh37 |
| NC_000002.10:g.122842815G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-24194G>A | ||
| XR_001739684.1:n.556-24194G>A |